Canonical Allele Identifier: CA2341125193

Gene: KLK2

Linked Data

• dbSNP Id: rs2090323752
• gnomAD v4: 19-50879722-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879722C>A , CM000681.2:g.50879722C>A	GRCh38
NC_000019.9:g.51382978C>A , CM000681.1:g.51382978C>A	GRCh37
NC_000019.8:g.56074790C>A	NCBI36
NG_031984.1:g.11290C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325321.8:c.*1163C>A MANE Select	ENSP00000313581.2:n.*1163C>A
ENST00000325321.7:c.*1163C>A	ENSP00000313581.2:n.*1163C>A
ENST00000358049.8:c.*1314C>A	ENSP00000350748.3:n.*1314C>A
ENST00000391810.6:c.*1163C>A	ENSP00000375686.2:n.*1163C>A
ENST00000597439.1:c.*1478C>A	ENSP00000471214.1:n.*1478C>A
NM_001002231.2:c.*1314C>A	NP_001002231.1:n.*1314C>A
NM_001256080.1:c.*1163C>A	NP_001243009.1:n.*1163C>A
NM_005551.4:c.*1163C>A	NP_005542.1:n.*1163C>A
NR_045762.1:n.2014C>A
NR_045763.1:n.2076C>A
NM_005551.5:c.*1163C>A MANE Select	NP_005542.1:n.*1163C>A
NM_001002231.3:c.*1314C>A	NP_001002231.1:n.*1314C>A
NR_045762.2:n.2008C>A
NR_045763.2:n.2070C>A
NM_001256080.2:c.*1163C>A	NP_001243009.1:n.*1163C>A